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Results: 1-4 |
Results: 4

Authors: Magre, J Delepine, M Khallouf, E Gedde-Dahl, T Van Maldergem, L Sobel, E Papp, J Meier, M Megarbane, A Lathrop, M Capeau, J
Citation: J. Magre et al., Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13, NAT GENET, 28(4), 2001, pp. 365-370

Authors: Delepine, M Nicolino, M Barrett, T Golamaully, M Lathrop, GM Julier, C
Citation: M. Delepine et al., EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome, NAT GENET, 25(4), 2000, pp. 406-409

Authors: Keavney, B McKenzie, C Parish, S Palmer, A Clark, S Youngman, L Delepine, M Lathrop, M Peto, R Collins, R
Citation: B. Keavney et al., Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls, LANCET, 355(9202), 2000, pp. 434-442

Authors: Farrall, M Keavney, B McKenzie, C Delepine, M Matsuda, F Lathrop, GM
Citation: M. Farrall et al., Fine-mapping of an ancestral recombination breakpoint in DCP1, NAT GENET, 23(3), 1999, pp. 270-271
Risultati: 1-4 |